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MANAGEMENT OF DIABETIC FOOT INFECTIONS & OSTEOMYELITIS DR. P.C. CHYE Consultant Orthopaedic Surgeon Dept. Orthopaedic Surgery & Traumatology Hospital Kuala Lumpur

Management of Foot SepsisOsteomyelitis

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  • MANAGEMENT OF DIABETIC FOOT INFECTIONS & OSTEOMYELITIS

    DR. P.C. CHYE Consultant Orthopaedic Surgeon Dept. Orthopaedic Surgery & Traumatology Hospital Kuala Lumpur

  • DIABETES MELLITUS

    Global Prevalence :

    2003 : 194 million

    2010 : 252 million

    2025 : 380 million

  • PREVALENCE OF DM IN MALAYSIA (Population >30 years)

    0.65%

    2.10%

    6.30%

    8.30%

    14.90%

    1960 1982 1986 1996 2006

    Year

    Prevalence of Diabetes Mellitus in Malaysia

    Prevalence

    3rd National Health and Mortality &

    Morbidity Survey

    22%

    08

  • DIABETIC FOOT INFECTIONS RISK FACTORS

    HOST DEFENSE : Neutrophil functions : chemotaxis,phagocytosis, intracellular killing Monocyte & complement functions PERIPHERAL VASCULAR DISEASES : in blood supply needed to heal ulcers and infection SENSORY NEUROPATHY : in appreciation of pain and temperature injuries not noticed, severity underestimated MOTOR NEUROPATHY : anatomical foot deformity abnormal pressure points

    ulceration AUTONOMIC NEUROPATHY : sweating, dry & cracked skin portal of bacteria entry

  • DIABETIC FOOT INFECTIONS - SPECTRUM

    Ranges from cellulitis to infected ulcers, abscess, osteomyelitis , wet gangrenes and necrotising fasciitis

  • 40% Mild 30-40% Moderate 20-30% Severe

    40-80% Infected

    (or suspected)

    15-25% Develop Foot Ulcer

    7% of Population

    Diabetic

    49% of diabetic patients with diabetic foot infection will develop infection in the other foot in 18 months

  • DIABETIC FOOT INFECTIONS THE DEVELOPMENT

    Usually precipitated by trauma

    Infection may start superficially in an ulcer or crack of the skin but can rapidly progress to involve deeper structures including tendons and bones

    The anatomical structures of various compartments of the foot, tendon sheaths, ligaments, fascia and neurovascular bundles tends to facilitate proximal spread of the infection

    Inflammation and infection in the foot compartments can cause compartment syndrome vascular thrombosis

  • DIABETIC FOOT INFECTIONS - PRESENTATIONS

    Redness, swelling, discharging sinus/ulcer, gangrene, pain

    Diabetic patient may or may not mount a fever, even in the presence of severe infection

    50% of patients with a limb-threatening infection do not manifest systemic signs or symptoms leading to underestimation of the presence and severity of infection

    The signs and symptoms are masked by neuropathy

    Hypotension, tachycardia and severe unexplained hyperglycaemia are however often noted

  • DIABETIC FOOT INFECTIONS - PROGRESSION

    Coexisting metabolic derangements, peripheral arterial disease, poor immune response poor delivery of antibiotics to the infected tissues, reduced access & functions of phagocytic cells to the infected area rapid progression of infection in hours or days & quickly become limb- or life-threatening

  • DIABETIC FOOT INFECTIONS

    These wounds are usually more severe & more complicated to treat than do equivalent infections in persons without diabetes

  • DIABETIC FOOT INFECTIONS - BACTERIA INVOLVED

    Aerobic Gram +ve cocci, esp (Staphylococcus aureus) are the predominant pathogens

    In chronic ulcers or in patients who have recently received antibiotic therapy may be infected with Gram ve rods

    In those with foot ischaemia and gangrene may have obligate anaerobic organisms

  • - Staphylococcus aureus 45%

    - Streptococcus sp. 35%

    - Enterococcus sp. 29%

    - Staphylococcus epidermidis 23%

    - Proteus mirabilis 26%

    - Pseudomonas aeruginosa 16%

    - Peptostreptococcus sp. 22%

    - Diphtheroids 19%

    - Bacteroides sp. 16%

  • Gram positive cocci

    Microbial complexity

    Microbial burden

    Clinical risk

    1 2 3 4

    Anaerobes

    Aerobic Gram-negative rods

    Prior Rx

    Necrosis

    Depth

    Severity

    Limb-threatening infections are often polymicrobial

  • MULTIRESISTANT BACTERIAL INFECTIONS

    Diabet Met 2004 Jul;21(7) : 710-5

    Diabetic foot ulcer and multidrug-resistant

    organisms: risk factors and impact. Hartemann-Heurtier A, Robert J, Jacqueminet S, Ha Van G, Golmard JL, Jarlier V, Grimaldi A.

    Detected in 1/3 of patients with

    previous history of hospital

    admission for the same wound

    Detected in 25% of patients

    with osteomyelitis

  • ALMOST 50% of Staph aureus isolated are MRSA !

    Clinical Microbiology & Infection- October 2005

    Prevalence of methicillin-resistant Staphylococcus aureus in infected and uninfected diabetic foot ulcers

  • TIMELINE OF STAPHYLOCOCCAL RESISTANCE

    1940 1950 1960 1970 1980 1990 2000 2010

    Penicillin-resistance

    GISA

    CA-MRSA

    VRSA

    Sporadic MRSA Epidemic MRSA

  • DIABETIC FOOT INFECTIONS TREATMENT STRTEGIES

    Require attention to both local & systemic issues

  • DIABETIC FOOT INFECTIONS -COMPREHENSIVE MANAGEMENT

    TREAT THE ULCER & INFECTION, GET THE WOUND TO HEAL, PREVENT RECURRENCE

    TREAT THE DIABETES, ASSOCIATED SYSTEMIC PROBLEMS & OVERCOME THE UNDERLYING PATHOLOGY

    LOC

    AL

    ISSU

    ES

    SYST

    EMIC

    ISSU

    ES

    +

    AT THE SAME TIME

  • DIABETIC FOOT INFECTIONS - MULTIDISCIPLINARY TEAM APPROACH

    Comprehensive management of these patients requires care of a finely-tuned multidisciplinary team for medical stabilization, surgical debridement, antibiotic selection, vascular reperfusion, wound care, podiatric care, orthotic care, nutrition support, rehabilitation and delayed reconstruction to achieve functional limb salvage

  • EVALUATION AT 3 LEVELS

    1 The patient as a whole 2 The affected limb or foot 3 The infected wound To determine : - presence, type, extent and severity of infection - pathogens involved - presence of any systemic consequences of infection - contribution of vascular disease / neuropathy - altered foot biomechanics that contributes to the cause of the wound ( and thus, its ability to heal )

  • DIABETIC FOOT INFECTIONS - INITIAL ASSESSMENT AND INVESTIGATIONS

    BLOOD INVESTIGATIONS : - Full blood count - Erythrocyte Sedimentation Rate (ESR) - C- Reactive Protein (CRP) - Random / Fasting Sugar Levels - Glycosylated Haemoglobin - Renal Profile - Serum Albumin

  • DIABETIC FOOT INFECTIONS - INITIAL ASSESSMENT AND INVESTIGATIONS

    EXAMINE THE FOOT : - Palpation/probing for fluctuance & tunneling wounds/ ulcer (deep

    infection) - a clinically infected ulceration probes to bone 89-95% osteomyelitis - Blood supply : Dorsalis Pedis , Posterior Tibialis & Popliteal pulses.

    Ankle-Brachial Systolic Index ( ABSI ), Doppler, Evidence of ischaemia & gangrene

    - the degree of impaired limb perfusion significantly reduce the chances of wound healing, increases the overall severity of infection and risk of amputations

    - Sensation --- Neuropathy pain in an insensate foot means severe infection

    - Deformities & Abnormal Pressure Points

  • DIABETIC FOOT INFECTIONS - INITIAL ASSESSMENT AND INVESTIGATIONS

    TAKE AN X-ray : - Osteomyelitis - Gas Gangrene - Presence of Foreign Body - Osseous deformities / fractures / dislocations MRI is more sensitive and specific, especially for extent of soft tissue involvement

  • DIABETIC FOOT INFECTIONS INITIAL MANAGEMENT

    IDENTIFY THE ORGANISMS INVOLVED : - Send appropriately obtained speciments for culture before

    starting empirical antibiotic therapy - Soft tissue or bone speciments obtained by biopsy, curettage, or

    aspiration are preferable - Superficial swab cultures of infected ulcers often complicate

    evaluation of the infection - Definitive antibiotic therapy will be based on C&S results from intra-op cultures

  • Initial treatment in a previously untreated patient with a non-limb-threatening infection is focused on Staphylococcus and Streptococcus sp

    Initial treatment of limb-threatening infections requires broad-spectrum antibiotics covering Staph aureus, group B Streps, other Streptococcus sp., enterobacteriaceae & anaerobes

    DIABETIC FOOT INFECTIONS INITIAL MANAGEMENT ANTIBIOTIC SELECTION

    Characteristic odours or history of resistant bacterial infections affect initial antibiotic choices

    Antibiotic vary in how well they achieve effective concentration in the infected diabetic foot -- affected by the arterial blood supply to the foot & pharmacodynamic properties of the drug

  • DIABETIC FOOT INFECTIONS INITIAL MEDICAL MANAGEMENT

    The degree of end organ dysfunction affects multiple aspects of medical and surgical management

    Antibiotic dosing adjustment issues, poor cardiac function, hyperglycaemia, ketoacidosis, dehydration, hyperosmolality, electrolyte imbalance, renal insufficiency, anaemia, poor limb perfusion, immunosuppression, poor nutrition, poor healing potential often coexist

    The goal of medical management is to regulate and normalize the metabolic and haemodynamic derangements and to prevent further decompensations

  • STABILIZE / RESUSCITATE THE PATIENT

    Restore fluid and electrolyte balances, correct anemia, hyperglycaemia,

    hyperosmolarity, acidosis &

    treat other exacerbating

    disorders

    Optimize treatment of other

    medical illnesses : ischaemic

    heart disease, heart failure,

    renal impairment etc

    May need resuscitation

    eg sepsis, ketoacidosis

  • DETERMINE THE NEED FOR SURGERY

    When a non-healing infected diabetic foot ulcer is worsening despite adequate wound care and cultured-directed antibiotics, urgent surgery is needed

    Emergency surgical intervention :

    Life- or limb-threatening infection

    eg. Necrotising fasciitis

    Gas gangrene

    Critical limb ischaemia

    Deep abscess

  • OVERVIEW OF SURGICAL MANAGEMENT OF INFECTED DIABETIC FOOT

    To achieve a healed wound & prevent

    major amputation of the leg :

    Darinage of pus, remove necrotic soft

    tissue & bone + creating a healthy

    wound bed

    Limb reperfusion

    Soft Tissue Cover

    Correct deformity, relieve pressure areas

    Restore stability, alignment & function

    Reduce risk of reulceration & subsequent amputation

    SUCCESSFUL SALVAGE

    Incision & drainage Debridement Sequestrectomy Disarticulation Ray Amputation

  • DIABETIC FOOT INFECTIONS INITIAL SURGICAL DEBRIDEMENT

    After patient is medically stabilised

    Must be timely and aggressive Remove all sloughs, necrotic and marginal-looking tissues, dead bones, drain all pus, explore all sinus tracts Exposed tendons should be excised if proximal migration of infection is suspected

    Exploration is done to determine involvement of fascial planes

    The degree of intra-operative bleeding must be assessed Aims to reduce the bacterial load in the wound, create a healthy environment

    to restore the physiologic processes of tissue repair and healing

    Changes stubborn non-healing chronic wounds into acute wounds

    Deep tissue & bone : C&S HPE ( if osteomyelitis suspected)

    Crucial to successful control of infection and must be done as soon as possible

    In severe infections, general anaesthesia is often needed as the depth of infection and fascial spread may be extensive

  • ANTIBIOTICS THERAPY

    OFTEN INSUFFICIENT WITHOUT APPROPRIATE WOUND CARE

    TREAT THE INFECTION, DO NOT STERILISE THE WOUND

    Based on culture & sensitivity results, depth and severity of infection CONTINUED UNTIL RESOLUTION OF INFECTION, NOT UNTIL THE WOUND HAS HEALED

  • DIABETIC FOOT INFECTIONS --- WOUND BED PREPARATION

    Converting a chronic wound into a wound with the potential to heal

    Involves debridement, control of infection and inflammation, moisture control, excision of wound edges and callus

    "TIME - "T" refers to the need to remove necrotic and diseased Tissue - "I" indicates the need to control bacterial burden and Infection - "M" refers to restoration of Moisture balance - "E" stands for the healing Edge, which is the point at which the wound is optimally primed for healing

  • DIABETIC FOOT INFECTIONS --REPEATED SHARP DEBRIDEMENT

    Repeated sharp debridement is done until all necrotic tissues and bone + biofilms are removed

    Stimulates production of growth factors and proliferation of collagen and fibroblasts

    A healthy wound bed is created for granulation tissue to grow and wound to heal

  • REPEATED DEBRIDEMENT - ULTRASONIC DEBRIDEMENT

    Use of low frequency cavitational ultrasound to debride away dead tissues, leaving healthy and granulation tissue intact

    Also removes bacteria and biofilms

    Sterile saline solution transfer the ultrasonic energy to the wound where tiny vibrating gas bubbles and cellular level fluid movement separates dead from healthy tissues

    Safe, cost effective , painless alternative to painful sharp debridements

    Low-frequency ultrasound has been shown to have cellular-level physical effects, known as cavitation and microstreaming, that can promote healing

    Cavitation is the formation and oscillation of microscopic bubbles, which expand and collapse as they resonate with the ultrasound frequency

    Acoustic microstreaming is the physical force of sound pressure waves that can displace small molecules and move fluids along and/or through cell membranes.

  • REPEATED DEBRIDEMENT - HYDROSURGICAL DEBRIDEMENT

    Versajet Hydrosurgery System ( Smith & Nephew) - utilises a high-pressure jet of sterile saline that travels

    parallel to the wound surface

    - This high-speed jet creates a Venturi effect that enables the surgeon to simultaneously hold, cut and remove tissue, while irrigating and aspirating the wound, with a single instrument

    Enables rapid debridement, likely to result in shorter procedure times

    Clean wounds potentially reduce the number of required debridement procedures

    Single device technique - combining lavage and sharp debridement instrumentation

    Multiple tip configurations enhance procedural flexibility

  • REPEATED DEBRIDEMENT - Maggots Debridement Therapy

    Sterile larva of the greenbottle fly is applied to the wound for 2-3 days

    Necrotic tissues are eaten away

    In late 1920s, William Baer from Johns Hopkins University, used maggots to treat children with osteomyelitis and soft tissue infections

    Successfully performed by thousands of physicians throughout 1930s, but was supplanted by the new antibiotics and surgical techniques during World War II

    In 2004, FDA allowed the production and marketing of the Phaenicia sericata larvae

    In 2006, approx 50,000 treatments were applied to wounds using maggots

    Low cost, simple, safe, ideal when surgical debridement is not the optimal choice

  • REPEATED DEBRIDEMENT - ENZYMATIC DEBRIDEMENT

    Involves application of a cream or ointment to the wound. The action of the chemicals or enzymes contained in the cream work to loosen the dead tissue, which is then manually removed Fast acting

    Minimal or no damage to healthy tissue with proper application.

    May be used as the primary technique for debridement in some cases when surgical debridement is not feasible owing to bleeding disorders or patient is not fit for surgery

    Combined therapy, such as initial surgical debridement followed by serial debridement using an enzymatic agent is effective for many patients with chronic, indolent, or nonhealing wounds

  • POST- DEBRIDEMENT SOFT TISSUE COVER

    Presence of large soft tissue defect after surgical debridement often makes primary closure difficult

    When possible, the least invasive methods of coverage are employed

    eg. Delayed primary closure

    Vacuum assisted closure

    However, many wounds are not amenable to delayed primary closure and require plastic surgical techniques

    - Split Skin Graft

    - Local and Pedicle Flaps

    - Free Flaps

  • VACUUM ASSISTED CLOSURE

    Using a vacuum source to draw fluid out of the wound to accelerate debridement and promote healing

    Not for acutely ischaemic foot, tumour wound

    Special precaution : patient on anticoagulant

    Wound bed preparation prior to initiation of treatment

    Optimal level of negative pressure ~125mmHg

    Most effective if applied in a cyclical pattern 5 mins on, 2 mins off

    Advantage : - cheap - Ideal for difficult- to heal wounds Disadvantages : - restricts patient mobility

  • DIABETIC FOOT INFECTIONS -- CELLULITIS

    9 times more frequent in diabetic compare to nondiabetic patients

    Infection is confined to the dermal and subcutaneous layers

    Commonly caused by Group A Streps & Staph

    Entry : skin cracks, fissures, blister, insect bites

    Antibiotics

  • DIABETIC FOOT INFECTIONS - OSTEOMYELITIS A difficult problem to treat & heal

    The combined effects of peripheral vascular disease, neuropathy, and repetitive trauma produce complex lesions with exposed bone, surrounding cellulitis, and soft tissue gangrene

    Plain x-rays, gallium scan, MRI

    Bone culture

  • DIABETIC FOOT INFECTIONS - OSTEOMYELITIS

    Diabetes Care August 2006 vol. 29 no. 8 1727-1732

    A Clinico-microbiological Study of Diabetic Foot Ulcers in an Indian

    Tertiary Care Hospital Ravisekhar Gadepalli, MSC; Benu Dhawan, MD; Vishnubhatla Sreenivas, PHD; Arti Kapil, MD1; A.C. Ammini, MD; Rama Chaudhry, MD

    All patients had Wagner 3-5 ulcers 62.5% had associated osteomyelitis

  • DIABETIC FOOT INFECTION - OSTEOMYELITIS

    If osteomyelitis is confirmed from initial deep cultures or histopathology, further aggressive resection of all affected bone is warranted

    DEBRIDE ALL DEAD BONE & SOFT TISSUE till viable, bleeding bone & soft tissue

    Staph aureus penetrates and survives in bone cells

    * BONE PENETRATION OF ANTIBIOTICS * Fluoroquinolones ( ciprofloxacin, ofloxacin, moxifloxacin), Fucidic acid

  • NECROTISING FASCIITIS IN DIABETIC

    Incidence on the rise

    70% of patients are diabetic

    MEDICAL & SURGICAL EMERGENCY !

    Highly fatal ( overall morbidity & mortality : 70-80% )

    Group A hemolytic streptococci ( Strep pyogenes ) and

    Staph aureus, alone or in synergism, are frequently the initiating infecting bacteria

    However, other aerobic and anaerobic pathogens may be present, including Bacteroides, Clostridium, Peptostreptococcus, Enterobacteriaceae, coliforms, Proteus, Pseudomonas, and Klebsiella.

    Poor prognostic factors : advanced age, poor glycaemic control, long duration of diabetes & delayed referral

  • NECROTISING FASCIITIS

  • Progressive, rapidly spreading infection along the deep fascia plane & extensive necrosis of the subcutaneous tissues & muscle without a corresponding necrosis of the overlying skin until much later

    Early features : Fever, pain, tachycardia, swelling, induration, cellulitis

    Late features : Severe pain & tenderness disproportionate to skin changes, skin discolouration ( purplish black ), blister or bullae, crepitus, septicaemic shock, multiorgan failure

    X-rays : subcutaneous gas

    Antibiotics

    Extensive surgical debridement & fasciotomy : delay for 24 hours mortality

  • THE ISCHAEMIC DIABETIC FOOT

    UNLESS THERE IS ADEQUATE REPERFUSION OF THE FOOT / LEG, ANTIBIOTICS TREATMENT

    AND SURGERY WILL FAIL & AMPUTATION WILL BE NEEDED

  • SURGERY IN THE DIABETIC FOOT

    Historically, diabetic foot surgery was largely done in the presence of acute infection or when in need of amputation

    With better understanding of the pathophysiology of diabetic foot disease, we have began to recognize the importance of elective diabetic foot surgery in helping patients to stay active and ulcer free

  • CLASSIFICATION OF SURGERY IN THE DIABETIC FOOT

    CLASS PURPOSE EXAMPLES I ( Elective ) For painful deformities in patients Realignment osteotomies, without neuropathy or open wounds tendon balancing procedures, II ( Prophylactic ) For prevention of ulceration in patients arthrodeses & Charcot with neuropathy but no open wounds reconstructions III ( Curative ) To assist healing of ulcers in patients Partial or complete removal of with neuropathy bone such as metatarsal head, sesamoid, accessory bone, exostosis, calcanectomy, soft tissue cover / reconstructions IV ( Emergent / To arrest / limit progression of acute Amputations, debridements, Ablative ) infection, eliminate infected and incision and drainage necrotic tissue Armstrong DG, Lavery LA, Frykberg RG. Validation of a diabetic foot surgery classification. Int Wound J 2006;3(3): 240-246

  • ELECTIVE & PROPHYLACTIC SURGERY FOR THE DIABETIC FOOT

    GOALS :

    1) Stability

    2) Realignment

    3) Platigrade foot amendable to bracing or accomodation

    4) Reduction of pressure points / surgical offloading

  • ELECTIVE / PROPHYLACTIC SURGERY

    FOREFOOT :

    HALLUX and FIRST METATARSALPHALANGEAL JOINT : - SESAMOIDECTOMY / EXOSTECTOMY

    - HALLUX INTERPHALANGEAL ARTHROPLASTY / ARTHRODESIS

    - RESECTION OF FIRST METATARSAL HEAD

    - OSTEOTOMIES OF THE PHALANX AND FIRST METATARSAL LESSER DIGITS : - LESSER METATARSAL OSTEOTOMIES : Shortening osteotomy Elevating osteotomy - LESSER METATARSAL HEAD RESECTION

  • ELECTIVE / PROPHYLACTIC SURGERY

    MIDFOOT :

    - EXOSTECTOMY

    - REALIGNMENT MIDFOOT OSTEOTOMIES + ARTHRODESIS

    - single plane vs multiplane

  • REARFOOT : - TRIPLE ARTHRODESIS

    - REALIGNMENT CALCANEAL OSTEOTOMIES

    - TALECTOMY + TIBIAL-CALCANEAL ARTHRODESIS

    - CALCANECTOMY ( partial / total )

  • OPTIMIZE THE HOST Correct and reverse all correctable negative factors on wound healing : - Anemia - Diabetes - Heart Failure - Malnutrition - Smoking - Steroid - Vitamin deficiency - Uraemia

  • FORMULATE A WOUND CARE PLAN Optimal wound care is crucial for healing but it is not the only way to treat the diabetic foot ulcer

    Infection complicates treatment of a diabetic foot ulcer, making a more aggressive wound care strategy necessary

    One particular dressing should not be used for all stages of wound

    A long process time, patience, perseverence -- Dedicated team of doctors and nurses Problems to be addressed in DFU : -- Exudate, bacterial load, slough, granulation

  • CHOOSING THE APPROPRIATE DRESSING

    INFECTED : surgical debridement + silver dressing

    EXUDATIVE : absorptive dressing

    eg. Hydrofibres, Alginates,

    Composite dressings,

    Foam dressings

    SLOUGHY : surgical / enzymatic /

    maggot debridement

    DRY : Hydrogels

  • SAVING EVERY LEG ? Reducing the number of lower extremity

    amputations is a goal for all doctors caring for patients with diabetes

    However, the numbers of limb-threatening infections continue to rise each year

    Failures in limb salvage attempts do occur

    These failures result in multiple trips to the operating room, significant potential morbidity and prolonged disability

  • AMPUTATION

    Somewhere in the world, a leg is lost to diabetes every 30 seconds

    Diabetics are 40x more likely to undergo amputation of the leg than non-diabetics

    >85 % of amputation begins with a foot ulcer

    Those who undergo a lower limb amputation have up to 30% chance of undergoing similar amputation on the contralateral limb within 3 years and up to 50% chance in 5 years

    Mortality rate post amputation: 11-41% after 1 year 20-50% after 3 years 39-68% after 5 years

    Two goals : ABLATION + RECONSTRUCTION

    refashioned the viable residual limb so that an appropriate prosthesis may be fitted to assist functional mobility

    AMPUTATION

  • STRAUSS WOUND GRADING SCORE

    VARIABLES 2 1.5 1 0.5 0

    PERFUSION

    DEPTH

    SIZE

    INFECTION

    WOUNDBASE

    Warm

    Skin & sub-Q

    < thumb

    Clean & contam.

    Red

    Cool

    Musc & tendons

    Thumb fist

    Cellulitis

    Yellow-white

    Cold

    Bone & Joint

    >fist

    Septic

    Black

    =8 0% amputation

  • MINOR AMPUTATIONS :

    - Disarticulation

    - Ray amputation

    - Midfoot amputation

    - Syme amputation

    MAJOR AMPUTATIONS :

    - Below knee amputation

    - Above knee amputation

    - Hip disarticulation

  • ENERGY CONSUMPTION AND AMPUTATION LEVEL

    AMPUTATION LEVEL % ENERGY BEYOND

    BASELINE

    Long BKA 10

    Medium BKA 25

    Short BKA 40

    Bilateral medium BKA

    41

    Average AKA 65

    Miller; Orthopaedic Review: Pg. 218.

  • AFTER AMPUTATION .

  • Specialty diabetic foot clinic : recurrence rate 25-80%/year

    Self-monitoring

    - to identify signs of disease and precursors to injury

    - many diabetic patients with a high risk for ulceration cannot see

    their feet ! ( obesity, limited joint mobility, visual impairment )

    - by the time patients in this study were able to visualize areas of

    concern, it was too late, and an ulceration had already developed

    Self-care

    CHALLENGE : PREVENTING RECURRENCE

  • CHALLENGE - PATIENTS

    EDUCATION & SUPPORT

    PERCEPTION & BEHAVIORAL

    CHANGE

    Overcoming : - Ignorance / Misconception - Fear - Denial - Uncooperativeness - Social problems

    Increase awareness of :

    - DM & its many consequences - Methods of care & support available

  • CHALLENGE THE OLD DIABETIC PATIENTS DIFFERENT FROM THE YOUNGER PATIENTS : Poorer limb perfusion

    Poorer healing / tissue regeneration

    Weaker immune defence

    Comorbidities ++

    Soft tissue fragility / osteoporosis

    Poor nutrition

    Poor vision / memory / senility

    Limited mobility

    Social and financial support problems

    Dependant, poor self care, neglect

    NURSING HOME PROBLEMS

    Two-thirds of elderly patients undergoing amputation do not return to independent life

  • CHALLENGE HEALTHCARE PERSONNEL

    Organisation : WOUND CARE TEAM - 70% of wound dressings are applied by the bedside

    nurse, NOT the wound care specialists

    Training ( Knowledge & Skills ) :

    - Train more people

    - Keep in touch with the latest development - Learn what to do, what not to do, how to do it

    Early detection & referral :

    - Educate & build a positive working relationaship with primary health care

    providers

    Budget & allocation

  • CHALLENGE HEALTH CARE SYSTEM

    Although there have been many advances in the management of

    the diabetic foot, it remained a major global public health

    problem

    Where have we failed ?

    Health Care Policy ?

    Health Care Budgeting ?

    Health Care Organisation ?

    Policy Implementation ?

    What needs to be done ? Present ? Future ?

    What about the poorer countries and their people ?

  • CHALLENGE - RESEARCH

    FROM THE BENCH TO THE BEDSIDE - integration of resources into a

    coordinated effort and monitoring

    pathway to bring products of research

    and technology to the patients

  • FUTURE OF DIABETIC WOUND CARE

    Narrowing gap between basic science and clinical application

    Necessary to understand the complex interactions of various physiologic components in wound healing

    SMART BIOACTIVE DRESSING -- that responds to the needs of the wound by releasing factors needed for healing

    STEM CELLS as a potentiator of healing by

    replacing or activating senescent cells in the wound eg. Bioengineered skin

  • OVERALL MANAGEMENT

    PREVENTION ! PREVENTION ! PREVENTION !

    Early detection and intervention

    Medical management of diabetes and comorbid conditions

    Targeted antibiotic coverage of infection

    TEAM EFFORT

    Wound care and dressing, off-loading / pressure relief

    Adjuvant therapies (eg. Hyperbaric O2 ) & Nutrition

    Post-op follow-up, podiatric care / foot wear and orthoses

    PREVENT RECURRENCE !

  • Doctor treating a foot ulcer : 17th Century, after David Teniers the younger

    THANK YOU